Pages that link to "Q48362804"

The following pages link to Congenital muscular dystrophy, white-matter abnormalities, and neuronal migration disorders: the expanding concept (Q48362804):

Displaying 7 items.

• The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review (Q24680748) ‎ (← links)
• The floppy infant: contribution of genetic and metabolic disorders (Q35226294) ‎ (← links)
• Tools for diagnosis of leukodystrophies and other disorders presenting with white matter disease (Q36060087) ‎ (← links)
• Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical cases. (Q41924831) ‎ (← links)
• Congenital muscular dystrophy in Israeli families. (Q44084332) ‎ (← links)
• Congenital muscular dystrophy in Arab children (Q45226643) ‎ (← links)
• Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models (Q98464776) ‎ (← links)